Canonical Allele Identifier: CA1467599768

Gene: ADAMTS3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313662_72313663delinsCA , CM000666.2:g.72313662_72313663delinsCA	GRCh38
NC_000004.11:g.73179379_73179380delinsCA , CM000666.1:g.73179379_73179380delinsCA	GRCh37
NC_000004.10:g.73398243_73398244delinsCA	NCBI36
NG_046955.1:g.260137_260138delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1745+14_1745+15delinsTG MANE Select	ENSP00000286657.4:n.1745+14_1745+15delinsTG
ENST00000286657.8:c.1745+14_1745+15delinsTG	ENSP00000286657.4:n.1745+14_1745+15delinsTG
ENST00000622135.1:c.1745+14_1745+15delinsTG	ENSP00000480055.1:n.1745+14_1745+15delinsTG
NM_014243.2:c.1745+14_1745+15delinsTG	NP_055058.2:n.1745+14_1745+15delinsTG
XM_011532421.1:c.1688+14_1688+15delinsTG	XP_011530723.1:n.1688+14_1688+15delinsTG
XM_011532422.1:c.1661+14_1661+15delinsTG	XP_011530724.1:n.1661+14_1661+15delinsTG
XM_011532423.1:c.1103+14_1103+15delinsTG	XP_011530725.1:n.1103+14_1103+15delinsTG
XM_011532424.1:c.1013+14_1013+15delinsTG	XP_011530726.1:n.1013+14_1013+15delinsTG
XM_011532421.2:c.1688+14_1688+15delinsTG	XP_011530723.1:n.1688+14_1688+15delinsTG
XM_011532422.3:c.1661+14_1661+15delinsTG	XP_011530724.1:n.1661+14_1661+15delinsTG
NM_014243.3:c.1745+14_1745+15delinsTG MANE Select	NP_055058.2:n.1745+14_1745+15delinsTG